Anaplasma phagocytophilum

Anaplasma phagocytophilum
Human HL60 cells containing Anaplasma phagocytophilum (indicated by arrows) which are basophilic intracytoplasmic inclusions when stained with Wright-Giemsa stain
Scientific classification edit
Domain: Bacteria
Phylum: Pseudomonadota
Class: Alphaproteobacteria
Order: Rickettsiales
Family: Ehrlichiaceae
Genus: Anaplasma
Species:
A. phagocytophilum
Binomial name
Anaplasma phagocytophilum
(Foggie 1949) Dumler et al. 2001[1]
Synonyms

Rickettsia phagocytophila ovis
Rickettsia phagocytophila
Cytoecetes phagocytophila
Cytoecetes phagocytophila

Anaplasma phagocytophilum (formerly Ehrlichia phagocytophilum)[2] is a Gram-negative bacterium that is unusual in its tropism to neutrophils. It causes anaplasmosis in sheep and cattle, also known as tick-borne fever and pasture fever, and also causes the zoonotic disease human granulocytic anaplasmosis.[3]

A. phagocytophilum is a Gram-negative, obligate bacterium of neutrophils. It causes human granulocytic anaplasmosis, which is a tick-borne rickettsial disease. Because this bacterium invades neutrophils, it has a unique adaptation and pathogenetic mechanism.[4]

Biology

A. phagocytophilum is a small, obligate, intracellular bacterium with a Gram-negative cell wall. It is 0.2–1.0 μm and lacks a lipopolysaccharide biosynthetic machinery. The bacterium first resides in an early endosome, where it acquires nutrients for binary fission and grows into small groups called morulae. This bacterium prefers to grow within myeloid or granulocytic cells.[4]

Hosts

Hosts include goat, cattle, horse and dog. Cattle infections had been suspected but were only first confirmed by Nieder et al. 2012.[5]

Bacterial mechanism

A. phagocytophilum binds to fucosylated and sialylated scaffold proteins on neutrophil and granulocyte surfaces. A type IV secretion apparatus is known to help in the transfer of molecules between the bacterium and the host. The most studied ligand is PSGL-1 (CD162). The bacterium adheres to PSGL-1 (CD162) through the 44-kDa major surface protein-2 (Msp2). After the bacterium enters the cell, the endosome stops maturation and does not accumulate markers of late endosomes or phagolysosomes. Because of this, the vacuole does not become acidified or fused to lysosomes. A. phagocytophilum then divides until cell lysis or when the bacteria leave to infect other cells.[4]

This bacterium has the ability to affect neutrophils by altering their function. It can survive the first encounter with the host cell by detoxifying superoxide produced by neutrophil phagocyte oxidase assembly. It also disrupts normal neutrophil function, such as endothelial cell adhesion, transmigration, motility, degranulation, respiratory burst, and phagocytosis.[4] It causes an increase in the secretion of IL-8, a chemoattractant that increases the phagocytosis of neutrophils. The purpose of this is to increase bacterial dissemination into the neutrophil.[6]

Role in human disease

a-d)Anaplasma phagocytophilum in human peripheral blood band neutrophil

A. phagocytophilum causes human granulocytic anaplasmosis (HGA). This disease was first identified in 1990, although this pathogen was known to cause veterinary disease since 1932. Since 1990, incidence of HGA has increased, and it is now recognized in Europe. This disease was first identified due to a Wisconsin patient who died with a severe febrile illness two weeks after a tick bite. During the last stage of the infection, a group of small bacteria was seen within the neutrophils in the blood. Other symptoms include fever, headache, absence of skin rash, leucopenia, thrombocytopenia, and mild injury to the liver.[4]

Diagnosis

These tests can be performed to determine an A. phagocytophilum infection:

  1. Indirect immunofluorescence assay is the principal test used to detect infection. The acute and convalescent phase serum samples can be evaluated to look for a four-fold change in antibody titer to A. phagocytophilum.
  2. Intracellular Inclusions (morulae) are visualized in granulocytes on Wright- or Giemsa- stained blood smears.
  3. Polymerase chain reaction assays are used to detect A. phagocytophilum DNA.[7]
Doxycycline

Treatment

Patients with HGA undergo doxycycline therapy, 100 mg twice daily until the patient's fever subsides for at least 3 days. This drug has been the most beneficial to those patients infected with the bacteria. Some other tetracycline drugs are also effective. In general, patients with symptoms of HGA and unexplained fever after a tick exposure should receive empiric doxycycline therapy while their diagnostic tests are pending, especially if they experience leukopenia and/or thrombocytopenia.[7]

In animals, antibiotics such as oxytetracycline, sulphamethazine, sulphadimidine, doxycycline, and trimethoprim-sulphonamides have been used.[3]

In animals

The disease is multisystemic, but the most severe changes are anaemia and leukopenia. This organism causes lameness, which can be confused with symptoms of Lyme disease, another tick-borne illness. It is a vector-borne zoonotic disease whose morula can be visualized within neutrophils (a type of white blood cell) from the peripheral blood and synovial fluid. It can cause lethargy, ataxia, loss of appetite, and weak or painful limbs.[3]

References

  1. ↑ "Page Anaplasma on lpsn.dsmz.de". Archived from the original on 2023-04-19. Retrieved 2023-04-17.
  2. ↑ Dumler JS, Barbet AF, Bekker CP, et al. (2001). "Reorganization of genera in the families Rickettsiaceae and Anaplasmataceae in the order Rickettsiales: unification of some species of Ehrlichia with Anaplasma, Cowdria with Ehrlichia and Ehrlichia with Neorickettsia, descriptions of six new species combinations and designation of Ehrlichia equi and 'HGE agent' as subjective synonyms of Ehrlichia phagocytophila". Int. J. Syst. Evol. Microbiol. 51 (Pt 6): 2145–65. doi:10.1099/00207713-51-6-2145. PMID 11760958.
  3. 1 2 3 Tick-Borne Fever Archived 2023-04-24 at the Wayback Machine reviewed and published by WikiVet, accessed 12 October 2011.
  4. 1 2 3 4 5 Dumler JS, Choi KS, Garcia-Garcia JC, et al. (December 2005). "Human granulocytic anaplasmosis and Anaplasma phagocytophilum". Emerging Infect. Dis. 11 (12): 1828–34. doi:10.3201/eid1112.050898. PMC 3367650. PMID 16485466.
  5. ↑ Brown, Wendy C.; Barbet, Anthony F. (2016-02-15). "Persistent Infections and Immunity in Ruminants to Arthropod-Borne Bacteria in the Family Anaplasmataceae". Annual Review of Animal Biosciences. Annual Reviews. 4 (1): 177–197. doi:10.1146/annurev-animal-022513-114206. ISSN 2165-8102. PMID 26734888.
  6. ↑ Thomas V, Fikrig E (July 2007). "Anaplasma phagocytophilum specifically induces tyrosine phosphorylation of ROCK1 during infection". Cell. Microbiol. 9 (7): 1730–7. doi:10.1111/j.1462-5822.2007.00908.x. PMID 17346310. S2CID 20043230.
  7. 1 2 "Human Anaplasmosis Information for Health Professionals: Diagnostic tests". Diseases. Minnesota Department of Health. Archived from the original on 2019-02-13. Retrieved 2011-04-27.
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